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16.72, 17.02, 18.29, 22.43, 25.69, 30.24, 36.17, 36.77, 37.15, 41.36, 49.77, 52.04, 67.33, 75.81, 106.84, 120.5, 125.99, 126.14, 131.17, 135.43, 135.83, 137.71, 142.39, 148.6, 166.08, 167.42, 169.56
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ÔìÒ¥Õß: ½ð±Ò+30, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2015-03-28 19:22:28
1 .     isoscalarafuran-A
    ÏàËÆ¶È:59.2%
Chinese Journal of Natural Medicines          2003          1          137-141
Sesterterpenoids from Marine Sponges Hyrtios erectus
QIU Yan; DENG Zhi-Wei; PEI Yue-Hu; FU Hong-Zheng; LIN Wen-Han
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2 .     isoscalarafuran-A
C27H40O4     ÏàËÆ¶È:59.2%
Australian Journal of Chemistry          1993          46          1295-1299
Two New Scalarane Sesterterpenes: Isoscalarafuran-A and -B, Epimeric Alcohols From a Southern Australian Marine Sponge, Spongia hispida
R Davis and RJ Capon
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
3 .     11-epi-carnosiflogenin C
C30H50O3     ÏàËÆ¶È:56.6%
Chemical & Pharmaceutical Bulletin          1988          36          234-243
Glycosides from Chinese Medicinal Plant, Hemsleya panacis-scandens, and Structure-Taste Relationship of Cucurbitane Glycosides
RYOJI KASAI,KAZUHIRO MATSUMOTO,RUI-LIN NIE,JUN ZHOU and OSAMU TANAKA
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
4 .     8-epi-Ophiobolin J
C25H36O4     ÏàËÆ¶È:55.5%
Phytochemistry          2006          67          2281-2287
Ophiobolin E and 8-epi-ophiobolin J produced by Drechslera gigantea,a potential mycoherbicide of weedy grasses
Antonio Evidente , Anna Andolfi, Alessio Cimmino, Maurizio Vurro, Mariano Fracchiolla, Raghavan Charudattan, Andrea Motta
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
5 .     7¦Á-acetyl-isopimara-8(14),15-dien-18-yl
C26H38O6     ÏàËÆ¶È:55.5%
Phytochemistry          1988          27          523-526
Terpenoids from Nepeta tuberosa subsp.reticulata (II)
J.G. Urones,I. Sanchez Marcos,J. Ferna¡ändez Ferreras,P. Basabe Barcala
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
6 .     Compound 7b
    ÏàËÆ¶È:55.5%
Bioorganic & Medicinal Chemistry Letters          2000          10          1815-1818
A concise synthesis of photoactivatable 4-Aroyl-L-phenylalanines
Enrico Morera, Giorgio Ortar
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
7 .     (2S,4aR,6aR,7R,9S,10aS,10bR)-methyl 9-acetoxy-2-(3-cyanobenzoyl)-6a,10b-dimethyl-4,10-dioxododecahydro-1H-benzo[f]isochromene-7-carboxylate
C27H27NO8     ÏàËÆ¶È:55.5%
Bioorganic & Medicinal Chemistry          2012          20          3100-3110
Semisynthetic neoclerodanes as kappa opioid receptor probes
Kimberly M. Lovell, Tamara Vasiljevik, Juan J. Araya, Anthony Lozama, Katherine M. Prevatt-Smith, Victor W. Day, Christina M. Dersch, Richard B. Rothman, Eduardo R. Butelman, Mary Jeanne Kreek, Thomas E. Prisinzano
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
8 .     (2S,4aR,6aR,7R,9S,10aS,10bR)-methyl 9-acetoxy-6a,10bdimethyl-4,10-dioxo-2-(3-(tri-fluoromethoxy)benzoyl)dodecahydro-1H-benzo[f]isochromene-7-carboxylate
C27H29F3O9     ÏàËÆ¶È:55.5%
Bioorganic & Medicinal Chemistry          2012          20          3100-3110
Semisynthetic neoclerodanes as kappa opioid receptor probes
Kimberly M. Lovell, Tamara Vasiljevik, Juan J. Araya, Anthony Lozama, Katherine M. Prevatt-Smith, Victor W. Day, Christina M. Dersch, Richard B. Rothman, Eduardo R. Butelman, Mary Jeanne Kreek, Thomas E. Prisinzano
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
9 .     4-Acetoxydictyolactone
C22H32O4     ÏàËÆ¶È:55.5%
The Journal of Organic Chemistry          1988          53          5010-5013
Antitumor xenicane and norxenicane lactones from the brown alga Dictyota dichotoma
Midori O. Ishitsuka, Takenori Kusumi, Hiroshi Kakisawa
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
10 .     Ophiobolin J
C25H38O4     ÏàËÆ¶È:55.5%
The Journal of Organic Chemistry          1988          53          2170-2172
Some new phytotoxic ophiobolins produced by Drechslera oryzae
Fumio Sugawara, Nobutaka Takahashi, Gary Strobel, Choong Hyo Yun, Gray George, Yali Fu, Jon Clardy
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
11 .     (3aR,4aS,5aR,6aR)-octahydro-5a-methyl-3-methylidene-5-((3E)-3-{[(3-nitrobenzoyl)oxy]imino}-butyl)-2H-cyclopropa[f][1]benzofuran-2-one
C22H24NNaO6     ÏàËÆ¶È:55.5%
Chemistry & Biodiversity          2014          11          886-903
Semisynthesis and Antifungal Activity of Novel Oxime Ester Derivatives of Carabrone Modified at C(4) against Botrytis cinerea
Delong Wang, Shuangxi Ren, Hao Wang, He Yan, Juntao Feng and Xing Zhang
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
12 .     (3aR,4aS,5aR,6aR)-octahydro-5a-methyl-5-((3E)-3-{[(3-methylbenzoyl)oxy)imino}butyl)-3-methylidene-2H-cyclopropa[f][1]benzofuran-2-one
C23H27NO4     ÏàËÆ¶È:55.5%
Chemistry & Biodiversity          2014          11          886-903
Semisynthesis and Antifungal Activity of Novel Oxime Ester Derivatives of Carabrone Modified at C(4) against Botrytis cinerea
Delong Wang, Shuangxi Ren, Hao Wang, He Yan, Juntao Feng and Xing Zhang
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
13 .     (3aR,4aS,5aR,6aR)-octahydro-5a-methyl-3-methylidene-5-((3E)-3-{[(naphthalen-2-ylacetyl)oxy]imino}butyl)-2H-cyclopropa[f][1]benzofuran-2-one
C27H29NO4     ÏàËÆ¶È:55.5%
Chemistry & Biodiversity          2014          11          886-903
Semisynthesis and Antifungal Activity of Novel Oxime Ester Derivatives of Carabrone Modified at C(4) against Botrytis cinerea
Delong Wang, Shuangxi Ren, Hao Wang, He Yan, Juntao Feng and Xing Zhang
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
14 .     (3aR,4aS,5aR,6aR)-octahydro-5a-methyl-3-methylidene-5-[(3E)-3-({[(2E)-3-(4-nitrophenyl)prop-2-enoyl]oxy}imino)butyl]-2H-cyclopropa[f][1]benzofuran-2-one
C24H26N2O6     ÏàËÆ¶È:55.5%
Chemistry & Biodiversity          2014          11          886-903
Semisynthesis and Antifungal Activity of Novel Oxime Ester Derivatives of Carabrone Modified at C(4) against Botrytis cinerea
Delong Wang, Shuangxi Ren, Hao Wang, He Yan, Juntao Feng and Xing Zhang
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
15 .     21-hydroxy-16-deacetyl-12-epi-scalarafuran acetate
C27H40O4     ÏàËÆ¶È:55.5%
Records of Natural Products          2014          4          417-421
Two New Scaralane-type Sesterterpenoids Isolated from the Marine Sponge Hyrtios erectus
Lu Yin, Hui Li, Xiaoling Chen and Yan Qiu
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
16 .     (2S,4aR,6aR,7R,9S,10aS,10bR)-methyl 9-acetoxy-2-(benzothiophene-2-carbonyl)-6a,10b-dimethyl-4,10-dioxododecahydro-1H-benzo[f]isochromene-7-carboxylate
C28H30O8S     ÏàËÆ¶È:53.5%
Bioorganic & Medicinal Chemistry          2012          20          3100-3110
Semisynthetic neoclerodanes as kappa opioid receptor probes
Kimberly M. Lovell, Tamara Vasiljevik, Juan J. Araya, Anthony Lozama, Katherine M. Prevatt-Smith, Victor W. Day, Christina M. Dersch, Richard B. Rothman, Eduardo R. Butelman, Mary Jeanne Kreek, Thomas E. Prisinzano
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
17 .     (2S,4aR,6aR,7R,9S,10aS,10bR)-methyl 9-acetoxy-2-(benzothiophene-3-carbonyl)-6a,10b-dimethyl-4,10-dioxododecahydro-1H-benzo[f]isochromene-7-carboxylate
C28H30O8S     ÏàËÆ¶È:53.5%
Bioorganic & Medicinal Chemistry          2012          20          3100-3110
Semisynthetic neoclerodanes as kappa opioid receptor probes
Kimberly M. Lovell, Tamara Vasiljevik, Juan J. Araya, Anthony Lozama, Katherine M. Prevatt-Smith, Victor W. Day, Christina M. Dersch, Richard B. Rothman, Eduardo R. Butelman, Mary Jeanne Kreek, Thomas E. Prisinzano
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
18 .     (1S,3aS,41R,4a1S,5R,10aS,12aS)-1-(furan-3-yl)-3,8-bis(hydroxy-imino)-4a1,7,7,10a,12a-pentamethyl-1,3,3a,4a1,5,6,6a,7,8,10a,10b,11,12,12a-tetradecahydronaphtho[2,1-f]oxireno[2,3-d]isochromen-5-yl acetate
C28H36N2O7     ÏàËÆ¶È:53.5%
Journal of Medicinal Chemistry          2008          51          6495-6502
Gedunin, a Novel Hsp90 Inhibitor: Semisynthesis of Derivatives and Preliminary Structure−Activity Relationships
Gary E. L. Brandt, Matthew D. Schmidt, Thomas E. Prisinzano and Brian S. J. Blagg
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
19 .     scabronine H
C27H36O5     ÏàËÆ¶È:51.8%
Helvetica Chimica Acta          2004          Vol. 87          2877
Isolation and Characterization of New Bitter Diterpenoids from the Basidiomycete Sarcodon scabrosus
Bing-Ji Ma, Hua-Jie Zhu, and Ji-Kai Liu
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
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